Congenital hypopituitarism: how to select the patients for genetic analyses

Aim of this commentary is to analyze the relationships between genotypic bases and phenotypic expression of congenital “multiple pituitary hormone deficiency” (MPHD) syndrome and to indicate some reliable criteria for selecting the patients who should undergo genetic analyses in order to clarify the...

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Detalles Bibliográficos
Autores principales: Crisafulli, Giuseppe, Aversa, Tommaso, Zirilli, Giuseppina, De Luca, Filippo, Gallizzi, Romina, Wasniewska, Malgorzata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889615/
https://www.ncbi.nlm.nih.gov/pubmed/29625578
http://dx.doi.org/10.1186/s13052-018-0484-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889615/
https://www.ncbi.nlm.nih.gov/pubmed/29625578
http://dx.doi.org/10.1186/s13052-018-0484-y

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